Literature DB >> 12182686

Issues in the conduct of therapeutic trials in palliative care: an Australian perspective.

Ian Maddocks1.   

Abstract

Palliative care has been slow to demonstrate that its common interventions are supported by high levels of evidence. There are multiple reasons for this--historical and cultural, as well as the recognised difficulties of conducting studies in dying persons. There are problems in isolating the effect of a single intervention from the many other changing dimensions which attend the progress of terminal illness, and problems also in defining particular outcomes free from the contaminating effect of other simultaneous changes in a patient's situation. Sickness is an interaction between disease and patient, and science sits more comfortably with the study of disease than with the understanding of the patient. Nevertheless, the therapies commonly employed for symptom management in individuals with advanced and terminal illness deserve more rigorous investigation to establish their efficacy. In Australia, new levels of government support for research have stimulated a closer examination of principles and practical guidelines for the conduct of research in this area of healthcare.

Entities:  

Keywords:  Biomedical and Behavioral Research; Death and Euthanasia

Mesh:

Year:  2002        PMID: 12182686     DOI: 10.2165/00002512-200219070-00003

Source DB:  PubMed          Journal:  Drugs Aging        ISSN: 1170-229X            Impact factor:   3.923


  23 in total

1.  Can it work? Does it work? Is it worth it? The testing of healthcareinterventions is evolving.

Authors:  B Haynes
Journal:  BMJ       Date:  1999-09-11

2.  Narrative and the practice of medicine.

Authors:  B Hurwitz
Journal:  Lancet       Date:  2000-12-16       Impact factor: 79.321

3.  The art and science of clinical knowledge: evidence beyond measures and numbers.

Authors:  K Malterud
Journal:  Lancet       Date:  2001-08-04       Impact factor: 79.321

4.  What investigations and procedures do patients in hospices want? Interview based survey of patients and their nurses.

Authors:  C J Meystre; N M Burley; S Ahmedzai
Journal:  BMJ       Date:  1997-11-08

5.  Consideration of consent in clinical research.

Authors:  P Speck
Journal:  Palliat Med       Date:  1996-04       Impact factor: 4.762

6.  The use and misuse of N-of-one studies.

Authors:  P C O'Brien
Journal:  Int J Oral Maxillofac Implants       Date:  1997 May-Jun       Impact factor: 2.804

7.  Multi-level models for repeated measurement data: application to quality of life data in clinical trials.

Authors:  H J Beacon; S G Thompson
Journal:  Stat Med       Date:  1996-12-30       Impact factor: 2.373

8.  Transdermal fentanyl versus sustained-release oral morphine in cancer pain: preference, efficacy, and quality of life. The TTS-Fentanyl Comparative Trial Group.

Authors:  S Ahmedzai; D Brooks
Journal:  J Pain Symptom Manage       Date:  1997-05       Impact factor: 3.612

9.  The number needed to treat: a clinically useful measure of treatment effect.

Authors:  R J Cook; D L Sackett
Journal:  BMJ       Date:  1995-02-18

10.  Will to live in the terminally ill.

Authors:  H M Chochinov; D Tataryn; J J Clinch; D Dudgeon
Journal:  Lancet       Date:  1999-09-04       Impact factor: 79.321

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